Reassembly of Unsaturated C–C Bonds by a Cutting/Insertion Cascade DOI
Yaojia Jiang, Ying Xu, Ling Li

и другие.

Synlett, Год журнала: 2022, Номер 34(04), С. 293 - 300

Опубликована: Ноя. 20, 2022

Abstract The reassembly of unsaturated C–C bonds has attracted widespread attention from synthetic chemists due to its advantages unique reactivity, easy handling, and high atom step economies. We recently explored a cutting/insertion cascade as means introducing new C1 source constructing functionalized 1,4-keto aldehyde 2H-furan derivatives through cyclopropanation enamines with various carbene precursors subsequent ring-opening reactions in situ. Aminocyclopropanes are believed be involved key intermediates these transformations. This Synpacts article outlines our recent contributions this increasingly important research area. 1 Introduction 2 Cleavage Enamine C=C Double Bonds Hydrolysis 1,4-Keto Aldehydes 3 Cyclization 2H-Furans 4 Ynone/Ynoate C≡C Triple 5 Conclusion

Язык: Английский

Catalytic ipso‐Nitration of Organosilanes Enabled by Electrophilic N‐Nitrosaccharin Reagent DOI Creative Commons
Ivan Mosiagin, Anthony J. Fernandes, Alena Budinská

и другие.

Angewandte Chemie, Год журнала: 2023, Номер 135(41)

Опубликована: Авг. 26, 2023

Abstract Nitroaromatic compounds represent one of the essential classes molecules that are widely used as feedstock for synthesis intermediates, preparation nitro‐derived pharmaceuticals, agrochemicals, and materials on both laboratory industrial scales. We herein disclose efficient, mild, catalytic ipso ‐nitration organotrimethylsilanes, enabled by an electrophilic N ‐nitrosaccharin reagent allows chemoselective nitration under mild reaction conditions, while exhibiting remarkable substrate generality functional group compatibility. Additionally, conditions proved to be orthogonal other common functionalities, allowing programming molecular complexity via successive transformations or late‐stage nitration. Detailed mechanistic investigation experimental computational approaches strongly supported a classical aromatic substitution (S E Ar) mechanism, which was found proceed through highly ordered transition state.

Язык: Английский

Процитировано

3

Iron-incorporated metal–organic frameworks for oxidative cleavage of trans-anethole to p-anisaldehyde DOI
Jun Xiong,

Xin Yuan,

Min‐Hua Zong

и другие.

Nanoscale, Год журнала: 2023, Номер 15(48), С. 19493 - 19498

Опубликована: Янв. 1, 2023

An iron-incorporated Zn-MOF catalyst Zn-bpydc·Fe was fabricated for the oxidative cleavage of trans-anethole to p-anisaldehyde under facile conditions, 1 atm O2. The Fe coordinated bipyridine serves as catalytically active center inside structural skeleton Zn-MOFs. This work affords a new avenue mild oxidation olefins.

Язык: Английский

Процитировано

1

Reassembly of Unsaturated C–C Bonds by a Cutting/Insertion Cascade DOI
Yaojia Jiang, Ying Xu, Ling Li

и другие.

Synlett, Год журнала: 2022, Номер 34(04), С. 293 - 300

Опубликована: Ноя. 20, 2022

Abstract The reassembly of unsaturated C–C bonds has attracted widespread attention from synthetic chemists due to its advantages unique reactivity, easy handling, and high atom step economies. We recently explored a cutting/insertion cascade as means introducing new C1 source constructing functionalized 1,4-keto aldehyde 2H-furan derivatives through cyclopropanation enamines with various carbene precursors subsequent ring-opening reactions in situ. Aminocyclopropanes are believed be involved key intermediates these transformations. This Synpacts article outlines our recent contributions this increasingly important research area. 1 Introduction 2 Cleavage Enamine C=C Double Bonds Hydrolysis 1,4-Keto Aldehydes 3 Cyclization 2H-Furans 4 Ynone/Ynoate C≡C Triple 5 Conclusion

Язык: Английский

Процитировано

1